苗勒氏管发育不全伴原发性闭经：一例表型正常女性的病例报告
Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female.
作者信息
Ajiboye Akinyosoye D, Omokanye Lukman O, Olatinwo Abdulwaheed O, Biliaminu Sikiru A
机构信息
Department of Obstetrics and Gynaecology, College of Health Sciences, University of Ilorin, Ilorin, Nigeria.
Department of Chemical Pathology and Immunology, College of Health Sciences, University of Ilorin, Ilorin, Nigeria.
出版信息
Saudi J Med Med Sci. 2017 May-Aug;5(2):160-162. doi: 10.4103/1658-631X.204859. Epub 2017 Apr 20.
Meyer-Rokitansky-Kuster-Hauser syndrome is a rare congenital abnormality occurring sporadically in females. It is the most common cause of primary amenorrhea. Affected persons usually appear normal on physical examination. This is a case of a 25-year-old woman who presented with primary amenorrhea and, subsequently, had diagnostic laparoscopy to confirm the diagnosis of Mullerian agenesis.
梅耶-罗基坦斯基-库斯特-豪泽综合征是一种罕见的先天性异常，散发于女性群体中。它是原发性闭经最常见的病因。患者在体格检查时通常外观正常。这是一例25岁女性患者，因原发性闭经前来就诊，随后接受了诊断性腹腔镜检查以确诊苗勒管发育不全。
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